List of variants in gene GRN reported by OMIM

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002087.4(GRN):c.*78C>T	rs5848	0.41298
NM_002087.4(GRN):c.1477C>T (p.Arg493Ter)	rs63751294	0.00001
NM_002087.4(GRN):c.2T>C (p.Met1Thr)	rs63751006	0.00001
NM_002087.3(GRN):c.1144dup (p.Thr382Asnfs)	rs63749905
NM_002087.4(GRN):c.-8+5G>C	rs63750313
NM_002087.4(GRN):c.102del (p.Gly35fs)	rs63751073
NM_002087.4(GRN):c.154del (p.Thr52fs)	rs63751092
NM_002087.4(GRN):c.26C>A (p.Ala9Asp)	rs63751243
NM_002087.4(GRN):c.373C>T (p.Gln125Ter)	rs63750077
NM_002087.4(GRN):c.388_391del (p.Gln130fs)	rs63749801
NM_002087.4(GRN):c.3G>A (p.Met1Ile)	rs63750331
NM_002087.4(GRN):c.675_676del (p.Ser226fs)	rs63751085
NM_002087.4(GRN):c.813_816del (p.Thr272fs)	rs63749877
NM_002087.4(GRN):c.835+1G>A	rs606231221
NM_002087.4(GRN):c.93_96dup (p.Asp33fs)	rs606231220
NM_002087.4(GRN):c.998del (p.Gly333fs)	rs63750873

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